ClinVar Miner

List of variants reported as likely benign for Darier disease

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_001681.3(ATP2A2):c.2860-5_2860-4delGT rs372303998
NM_170665.4(ATP2A2):c.*3823A>C rs193112984
NM_170665.4(ATP2A2):c.*4047A>G rs75547854
NM_170665.4(ATP2A2):c.*4578G>A rs143926209
NM_170665.4(ATP2A2):c.*4580C>T rs9540
NM_170665.4(ATP2A2):c.-10C>G rs201929640
NM_170665.4(ATP2A2):c.-15C>T rs373966549
NM_170665.4(ATP2A2):c.-240G>A rs577127824
NM_170665.4(ATP2A2):c.-274G>C rs558822961
NM_170665.4(ATP2A2):c.-324G>A rs543056549
NM_170665.4(ATP2A2):c.-500T>C rs550888717
NM_170665.4(ATP2A2):c.1096-12C>G rs138711897
NM_170665.4(ATP2A2):c.1167T>C (p.Tyr389=) rs115016152
NM_170665.4(ATP2A2):c.1323A>G (p.Thr441=) rs148550709
NM_170665.4(ATP2A2):c.137-12T>C rs376032579
NM_170665.4(ATP2A2):c.2058C>T (p.Ile686=) rs140766323
NM_170665.4(ATP2A2):c.2319-12G>A rs369489819
NM_170665.4(ATP2A2):c.2628A>G (p.Lys876=) rs149324360
NM_170665.4(ATP2A2):c.2945C>T (p.Thr982Met) rs149024535
NM_170665.4(ATP2A2):c.327A>G (p.Glu109=) rs55984131
NM_170665.4(ATP2A2):c.81A>G (p.Glu27=) rs3026434
NM_170665.4(ATP2A2):c.94C>T (p.Leu32Phe) rs141335001

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